Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4763
Gene Symbol: NF1
NF1
1.000 Biomarker disease GENOMICS_ENGLAND The RASopathies. 23875798 2013
Entrez Id: 867
Gene Symbol: CBL
CBL
0.800 Biomarker disease GENOMICS_ENGLAND Germline Genetic Predisposition to Hematologic Malignancy. 28297620 2017
Entrez Id: 23092
Gene Symbol: ARHGAP26
ARHGAP26
0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 171023
Gene Symbol: ASXL1
ASXL1
0.600 Biomarker disease GENOMICS_ENGLAND Recent advances in understanding clonal haematopoiesis in aplastic anaemia. 28107566 2017
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 GeneticVariation disease UNIPROT Determination of the catalytic activity of LEOPARD syndrome-associated SHP2 mutants toward parafibromin, a bona fide SHP2 substrate involved in Wnt signaling. 26742426 2016
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 GeneticVariation disease UNIPROT Functional analyses documented that the two most common mutations in PTPN11 associated with JMML caused a gain of function. 12717436 2003
Entrez Id: 3845
Gene Symbol: KRAS
KRAS
1.000 GeneticVariation disease UNIPROT Of 11 children with juvenile myelomonocytic leukemia (JMML) carrying RAS mutations (8 with NRAS mutations, 3 with KRAS2 mutations), 5 had a profound elevation in either or both the white blood cells and spleen size at diagnosis. 17332249 2007
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.800 GeneticVariation disease UNIPROT Of 11 children with juvenile myelomonocytic leukemia (JMML) carrying RAS mutations (8 with NRAS mutations, 3 with KRAS2 mutations), 5 had a profound elevation in either or both the white blood cells and spleen size at diagnosis. 17332249 2007
Entrez Id: 26040
Gene Symbol: SETBP1
SETBP1
0.550 GeneticVariation disease UNIPROT Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia. 23832011 2013
Entrez Id: 4763
Gene Symbol: NF1
NF1
1.000 SomaticCausalMutation disease ORPHANET Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. 19571318 2009
Entrez Id: 3845
Gene Symbol: KRAS
KRAS
1.000 SomaticCausalMutation disease ORPHANET Juvenile myelomonocytic leukemia (JMML) is an intractable pediatric leukemia with poor prognosis whose molecular pathogenesis is poorly understood, except for somatic or germline mutations of RAS pathway genes, including PTPN11, NF1, NRAS, KRAS and CBL, in the majority of cases. 23832011 2013
Entrez Id: 3845
Gene Symbol: KRAS
KRAS
1.000 SomaticCausalMutation disease ORPHANET Molecular basis of juvenile myelomonocytic leukemia. 20139388 2010
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 SomaticCausalMutation disease ORPHANET Ptpn11(E76K) mutation is the most common and most active Ptpn11 mutation found in JMML and acute leukemias. 21930766 2011
Entrez Id: 4763
Gene Symbol: NF1
NF1
1.000 SomaticCausalMutation disease ORPHANET Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia. 23832011 2013
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 SomaticCausalMutation disease ORPHANET Molecular basis of juvenile myelomonocytic leukemia. 20139388 2010
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 SomaticCausalMutation disease ORPHANET Juvenile myelomonocytic leukemia (JMML) is an intractable pediatric leukemia with poor prognosis whose molecular pathogenesis is poorly understood, except for somatic or germline mutations of RAS pathway genes, including PTPN11, NF1, NRAS, KRAS and CBL, in the majority of cases. 23832011 2013
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 SomaticCausalMutation disease ORPHANET Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. 19571318 2009
Entrez Id: 4763
Gene Symbol: NF1
NF1
1.000 SomaticCausalMutation disease ORPHANET Molecular basis of juvenile myelomonocytic leukemia. 20139388 2010
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.800 SomaticCausalMutation disease ORPHANET Juvenile myelomonocytic leukemia (JMML) is an intractable pediatric leukemia with poor prognosis whose molecular pathogenesis is poorly understood, except for somatic or germline mutations of RAS pathway genes, including PTPN11, NF1, NRAS, KRAS and CBL, in the majority of cases. 23832011 2013
Entrez Id: 867
Gene Symbol: CBL
CBL
0.800 SusceptibilityMutation disease ORPHANET Juvenile myelomonocytic leukemia (JMML) is an intractable pediatric leukemia with poor prognosis whose molecular pathogenesis is poorly understood, except for somatic or germline mutations of RAS pathway genes, including PTPN11, NF1, NRAS, KRAS and CBL, in the majority of cases. 23832011 2013
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.800 SomaticCausalMutation disease ORPHANET Molecular basis of juvenile myelomonocytic leukemia. 20139388 2010
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.800 SomaticCausalMutation disease ORPHANET The clinical course of these patients suggests that NRAS mosaicism may be associated with a mild disease phenotype in JMML. 22753870 2012
Entrez Id: 6237
Gene Symbol: RRAS
RRAS
0.510 GeneticVariation disease ORPHANET We also identified somatic RRAS mutations (p.Gly39dup and p.Gln87Leu) in 2 of 110 cases of non-syndromic juvenile myelomonocytic leukaemia, a childhood myeloproliferative/myelodysplastic disease caused by upregulated RAS signalling, defining an atypical form of this haematological disorder rapidly progressing to acute myeloid leukaemia. 24705357 2014
Entrez Id: 4763
Gene Symbol: NF1
NF1
1.000 Biomarker disease HPO
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
1.000 Biomarker disease HPO